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XB-GENEPAGE-853647
foxj1 forkhead box J1
Anatomical Phenotypes
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abnormal ciliated epidermal cell (2 sources), abnormally decreased number of ciliated epidermal cell (2 sources), abnormally decreased number of multiciliated epidermal cell (2 sources) |
Expression Phenotypes
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Manual annotations: foxj1 manipulated (7 sources), foxj1 assayed (18 sources) |
Computed annotations: foxj1 assayed (19 sources) |
Diseases
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allergic rhinitis (1AP source), autoimmune disease (1AP source), situs inversus (1 EP source), visceral heterotaxy (1 EP source) |
Experiments (Reagents)
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Xla Wt + foxj1 (1 source), Xla Wt + foxj1 (1 source), Xla Wt + foxj1 (1 source), Xla Wt + foxj1 CRISPR (1 source), Xla Wt + foxj1 CRISPR (1 source), Xla Wt + foxj1 MO (1 source), Xla wt + foxj1 sgnRNA1 CRISPR (1 source), Xtr Wt + foxj1 CRISPR (1 source), Xtr Wt + foxj1 MO (1 source) |
Monarch Ortholog Phenotypes
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Human (35 sources): Abnormality of the digestive system, Abnormality of the immune system, Airway obstruction, Asplenia, Asthma, Atelectasis, Bronchiectasis, Chronic bronchitis, Chronic otitis media, Chronic sinusitis, [+] |
Mouse (36 sources): abnormal brain development, abnormal brain ependyma morphology, abnormal brain ventricle morphology, abnormal choroid plexus morphology, abnormal embryonic cilium location or orientation, abnormal left-right axis patterning, abnormal neuron differentiation, abnormal olfactory bulb development, abnormal postnatal subventricular zone morphology, abnormal primitive node morphology, [+] |
View all ortholog results at Monarch |